A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703118



Internal ID15093084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112593202..112616506hg38UCSC Ensembl
Innerchr10:114352961..114376265hg19UCSC Ensembl
Innerchr10:114342951..114366255hg18UCSC Ensembl
Innerchr10:114342951..114366255hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3823305
hg1923305
hg1823305
hg1723305
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526766
Supporting Variants
Samples
Known GenesVTI1A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703118
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer